Product description

DS Maref LX9 Sequential Pneumatic Compression Device

Serial numbers: 220112944 to 20117954 and 2026322 to 2032792

ARTG 206228
(Medi-Rent Pty Ltd - Compression unit, sequential)

Sequential Intermittent Pneumatic Compression (SIPC) therapy is the process of applying external pressure to the limbs to promote the circulation of blood and lymphatic fluid from the extremities of the body.

See a list of details to help identify the product

Reason the product is recalled

A fault in the programming of the LX9 pumps, may cause users to experience higher pressure in the garments than set on the device.

The hazards to consumers

If the pressure in the garments becomes excessive for the user and exceeds the devices pressure specifications, this could result in an increased risk of health complications.

What consumers should do

Medi-Rent will update the programming on all pumps which have been programmed with software version 2020.11.01, which will correct the issue.

In the interim, consumers are advised to follow the instructions in the customer letter for use of the device until the reprogramming is complete.

For further information, contact Medi-Rent by phone on 1300 726 666.

Details to help identify the product

Supplier running the recall

Who sold the product

Hospital and health services in ACT, NSW, SA, Qld, Vic and WA

Where the product was sold

International
Online
New South Wales
Queensland
South Australia
Victoria
Western Australia
Australian Capital Territory

Responsible regulators

Regulators are established or appointed by government. They enforce regulations and rules.

Quote PRA number 2021/19283 when contacting a regulator about this recall.

Recall and remedy questions

Contact the Therapeutic Goods Administration if you have:

  • a question about the remedy being offered to you by the business that is responsible for managing this recall, or
  • concerns about the way the business is managing this recall.